OBJECTIVE: To assess the relationship of levels of inflammatory risk markers to presence of clinical coronary artery disease (CAD) in patients with treated heterozygous familial hypercholesterolaemia. DESIGN: A cross-sectional study of patients on the Simon Broome Familial Hyperlipidaemia Register. SETTING: Six hospital outpatient clinics in the UK. PARTICIPANTS: A total of 211 men and 199 women with heterozygous familial hypercholesterolaemia. MAIN OUTCOME MEASURES: Analysis of conventional risk factors and concentrations of high-sensitivity C-reactive protein (hsCRP), lipoprotein(a), serum intercellular adhesion molecule (sICAM), interleukin-6 (IL-6) and lipoprotein-associated phospholipase A2 (LpPLA2) mass. RESULTS: CAD was present in 10...
Abstract Background Familial hypercholesterolaemia (FH) leads to premature coronary artery diseases ...
© 2017 National Lipid Association Background Familial hypercholesterolemia (FH) is the most common a...
International audienceBackground and Aim: Lipoprotein-associated phospholipase A2 (Lp-PLA2) plays a ...
OBJECTIVES: To assess the clinical and biochemical factors associated with inter-individual variatio...
BACKGROUND: Heterozygous familial hypercholesterolemia (hFH) and familial combined hyperlipidemia (F...
Background: The European Atherosclerosis Society Familial Hypercholesterolaemia Studies Collaboratio...
Background: The European Atherosclerosis Society Familial Hypercholesterolaemia Studies Collaboratio...
Familial Hypercholesterolaemia (FH) is a genetic disorder leading to an increase in levels of total ...
Background: Familial hypercholesterolemia (FH) is a common autosomal dominant disorder caused by mu...
Familial hypercholesterolemia (FH) is an autosomal dominant disorder in which the primary defect is ...
Background: Heterozygous Familial hypercholesterolemia (FH) is a common autosomal d...
Background and aims: Familial hypercholesterolaemia (FH) is a powerful risk factor for cardiovascula...
Author: Gintarė Valterytė Title: Identification of Patients with Familial Hypercholesterolemia (FH) ...
Abstract Background Familial hypercholesterolaemia (FH) leads to premature coronary artery diseases ...
© 2017 National Lipid Association Background Familial hypercholesterolemia (FH) is the most common a...
International audienceBackground and Aim: Lipoprotein-associated phospholipase A2 (Lp-PLA2) plays a ...
OBJECTIVES: To assess the clinical and biochemical factors associated with inter-individual variatio...
BACKGROUND: Heterozygous familial hypercholesterolemia (hFH) and familial combined hyperlipidemia (F...
Background: The European Atherosclerosis Society Familial Hypercholesterolaemia Studies Collaboratio...
Background: The European Atherosclerosis Society Familial Hypercholesterolaemia Studies Collaboratio...
Familial Hypercholesterolaemia (FH) is a genetic disorder leading to an increase in levels of total ...
Background: Familial hypercholesterolemia (FH) is a common autosomal dominant disorder caused by mu...
Familial hypercholesterolemia (FH) is an autosomal dominant disorder in which the primary defect is ...
Background: Heterozygous Familial hypercholesterolemia (FH) is a common autosomal d...
Background and aims: Familial hypercholesterolaemia (FH) is a powerful risk factor for cardiovascula...
Author: Gintarė Valterytė Title: Identification of Patients with Familial Hypercholesterolemia (FH) ...
Abstract Background Familial hypercholesterolaemia (FH) leads to premature coronary artery diseases ...
© 2017 National Lipid Association Background Familial hypercholesterolemia (FH) is the most common a...
International audienceBackground and Aim: Lipoprotein-associated phospholipase A2 (Lp-PLA2) plays a ...